Abstract |
The dose of orally administered 9-deazainosine calculated to suppress 50% of Leishmania donovani amastigotes in hamster livers was 19 mg/kg ( body weight) per day; 96 to 99% of Leishmania organisms were eliminated from the liver and spleen of squirrel monkeys by 50 mg/kg per day. Because these activities were greater than that of the experimental clinical agent allopurinol and comparable to that of the classical agent parenteral pentavalent antimony, 9-deazainosine should be considered for clinical development for visceral leishmaniasis.
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Authors | J D Berman, W L Hanson, J K Lovelace, V B Waits, J E Jackson, W L Chapman Jr, R S Klein |
Journal | Antimicrobial agents and chemotherapy
(Antimicrob Agents Chemother)
Vol. 31
Issue 1
Pg. 111-3
(Jan 1987)
ISSN: 0066-4804 [Print] United States |
PMID | 3566235
(Publication Type: Journal Article)
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Chemical References |
- Formycins
- Organometallic Compounds
- Guanosine
- 3-deazaguanosine
- Inosine
- Allopurinol
- Meglumine
- Meglumine Antimoniate
- 9-deazainosine
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Topics |
- Administration, Oral
- Allopurinol
(administration & dosage, pharmacology)
- Animals
- Cricetinae
- Formycins
(administration & dosage, pharmacology)
- Guanosine
(administration & dosage, analogs & derivatives, pharmacology)
- Injections, Intramuscular
- Inosine
(administration & dosage, analogs & derivatives, pharmacology)
- Leishmania donovani
(drug effects)
- Leishmaniasis, Visceral
(drug therapy, parasitology)
- Liver
(parasitology)
- Male
- Meglumine
(administration & dosage, pharmacology)
- Meglumine Antimoniate
- Mesocricetus
- Organometallic Compounds
(administration & dosage, pharmacology)
- Saimiri
- Spleen
(parasitology)
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